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TitleDESIGN OF WEAKLY BASIC THROMBIN INHIBITORS INCORPORATING NOVEL P1 BINDING FUNCTIONS: MOLECULAR AND X-RAY CRYSTALLOGRAPHIC STUDIES
Journal, issue, pagesBiochemistry, Vol. 42, Page 9013-9021, Year 2003
Publish dateJan 16, 2003 (structure data deposition date)
AuthorsDe Simone, G. / Menchise, V. / Omaggio, S. / Pedone, C. / Scozzafava, A. / Supuran, C.T.
External linksBiochemistry / PubMed:12885234
MethodsX-ray diffraction
Resolution1.9 Å
Structure data

PDB-1no9:
Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.
Method: X-RAY DIFFRACTION / Resolution: 1.9 Å

Chemicals

ChemComp-NAG:
2-acetamido-2-deoxy-beta-D-glucopyranose

ChemComp-4ND:
N4-(N,N-DIPHENYLCARBAMOYL)-AMINOGUANIDINE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • hirudo medicinalis (medicinal leech)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / COMPLEX (SERINE PROTEASE-INHIBITOR) / BLOOD COAGULATION / SERINE PROTEINASE INHIBITION / N / N-DIPHENYLCARBAMOYL-AMINOGUANIDINE / HYDROLASE / HYDROLASE-HYDROLASE INHIBITOR COMPLEX

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